Lv2
110 积分 2024-11-20 加入
High prevalence of neonatal presentation in Korean patients with citrullinemia type 1, and their shared mutations
13天前
已完结
Clinical utility of expanded carrier screening in the preconception and prenatal population: A Chinese cohort study
1个月前
已完结
Clinical implications of expanded carrier screening for pregnancy-related care and individual health
1个月前
已完结
Integrated Genotyping Strategies for Uncovering Detailed Haplotype Structures and Characterization of DMD Duplications
1个月前
已完结
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
1个月前
已完结
Single-center experience using reflex-targeted next-generation sequencing at diagnosis of squamous cell lung carcinoma in daily practice
2个月前
已关闭
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity
8个月前
已完结
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